Allele Registry

Canonical Allele Identifier: PA2829743388

Gene: BBS9 HGNC NCBI

ClinVar RCV:

RCV002716319

RCV003916520

ClinVar Variation:

1963991

HGVS (amino-acid)	Matching Registered Transcripts
NP_055266.2:p.Arg7Ser	CA4213850 NM_014451.4:c.19C>A